PRESS RELEASE published on 09/03/2025 at 07:00, 11 months 5 days ago Valneva annonce de nouvelles données positives d’innocuité et d’immunogénicité de Phase 2 pour le candidat vaccin contre la maladie de Lyme Valneva annonce des données positives d'innocuité et d'immunogénicité de Phase 2 pour le vaccin VLA15 contre la maladie de Lyme, avec forte réponse immunitaire chez les enfants et les adultes Valneva Maladie De Lyme Vaccin Innocuité Immunité
BRIEF published on 08/26/2025 at 11:30, 11 months 13 days ago Perspectives boursières de Valneva face aux défis réglementaires Valneva SE Maladie De Lyme Vaccin Contre Le Chikungunya Marché Des Vaccins Suspension De La FDA
BRIEF published on 08/26/2025 at 11:30, 11 months 13 days ago Valneva's Stock Outlook Amid Regulatory Challenges Valneva SE Lyme Disease Chikungunya Vaccine Vaccine Market FDA Suspension
PRESS RELEASE published on 08/26/2025 at 11:25, 11 months 13 days ago Original-Research: Valneva SE (von First Berlin Equity Research GmbH): Buy First Berlin Equity Research updates Valneva SE (ISIN: FR0004056851) with BUY rating & reduced target price to EUR 6.30. FDA suspends Valneva's chikungunya vaccine; VLA15 Lyme disease vaccine prospects remain positive First Berlin Equity Research BUY Rating Valneva SE Chikungunya Vaccine Lyme Disease VLA15
BRIEF published on 08/25/2025 at 07:05, 11 months 14 days ago Suspension par la FDA de la licence d'IXCHIQ® aux États-Unis FDA Suspension Vaccin Chikungunya IXCHIQ®
BRIEF published on 08/25/2025 at 07:05, 11 months 14 days ago FDA suspends IXCHIQ® license in the United States FDA Suspension Vaccine Chikungunya IXCHIQ®
PRESS RELEASE published on 08/25/2025 at 07:00, 11 months 14 days ago Valneva Announces FDA’s Decision to Suspend License of Chikungunya Vaccine IXCHIQ® in the U.S. Valneva SE announces FDA's suspension of IXCHIQ® chikungunya vaccine license in the U.S. due to serious adverse events, despite reported cases consistent with clinical trials. Sales impact to be evaluated FDA Valneva SE Chikungunya Vaccine License Suspension Serious Adverse Events
PRESS RELEASE published on 08/25/2025 at 07:00, 11 months 14 days ago Valneva annonce la décision de la FDA de suspendre la licence d’IXCHIQ® aux États-Unis La FDA suspend la licence d'IXCHIQ® aux États-Unis en raison d'effets indésirables graves liés au chikungunya. Valneva analyse les cas et reste engagée à assurer la sécurité des vaccins FDA Valneva Suspension Chikungunya IXCHIQ
BRIEF published on 08/19/2025 at 10:44, 11 months 20 days ago First Berlin Maintains Buy Rating for Valneva Amid Strong Q2 Results BUY Rating Q2 Results Valneva SE Lyme Disease Vaccine Chikungunya Vaccine
BRIEF published on 08/19/2025 at 10:44, 11 months 20 days ago First Berlin maintient sa recommandation d'achat sur Valneva malgré de solides résultats au deuxième trimestre Valneva SE Acheter Une Note Vaccin Contre La Maladie De Lyme Résultats Du Deuxième Trimestre Vaccin Contre Le Chikungunya
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